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1.
Five pigeons pecked lighted keys for food reinforcers delivered by several multiple variable interval 2-min variable interval 2-min schedules. At different times, the components of the multiple schedule both supplied food reinforcers, both supplied water, or one supplied food and the other supplied water. Rates of responding during the water component of the food-water schedule were lower than the rates during comparable components of the water-water schedules (negative contrast). But, the rates of responding during the food component of the food-water schedule were not greater than the rates of responding during comparable components of the food-food schedules (absence of positive contrast) at two different levels of water deprivation. These results raise questions about several theories of behavioral contrast, and they may restrict the scope of any theory that attributes positive and negative contrast to symmetrical factors. 相似文献
2.
Frances K. McSweeney 《Learning & behavior》1992,20(2):160-169
Rats pressed levers for Noyes pellets or keys for sweetened condensed milk reinforcers delivered by multiple schedules. Session length and baseline rates of reinforcement were varied in two experiments. Rates of responding increased during the early part of the session and then decreased for both responses and reinforcers, as well as for all subjects and values of the independent variables. Changes in response rates across the session sometimes exceeded 500%. Respoiise rates peaked approximately 20 min after the beginning of the session, regardless of session duration, when subjects responded on a multiple variable interval 1-min variable interval 1-min schedule. The function was flatter for longer sessions than it was for shorter sessions. The function was flatter, more symmetrical, and peaked later for lower rates of reinforcement than for higher rates of reinforcement. The function appeared early in training, and further experience moved and reduced its peak. Variables related to reinforcement exerted more control over some aspects of this function than did variables related to responding. These within-session patterns of responding may have fundamental implications for experimental design and theorizing. 相似文献
3.
Pigeons were studied on multiple variable-ratio yoked-variable-interval schedules in which components had equal rates of food reinforcement and appeared equally often on each of two keys. Interpolated between component changes on the final multiple schedule were 10-sec probes in which both schedule stimuli were present, one on each key. During multiple schedule training, variable-ratio response rates were greater than yoked-variable-interval rates; however, response rate differences in the components were not a function of the mean ratio value for the 40-to-320-ratio range studied. During the choice probes, subjects responded more to the stimulus associated with the interval schedule than to the one associated with the ratio schedule. It was concluded that pigeons prefer interval schedules over equal reinforcement rate ratio schedules, because the former generate fewer responses per reinforcement. 相似文献
4.
The effects of different schedule requirements at reinforcement on patterns of responding by pigeons were assessed under conjunctive schedules with comparable response-number requirements, Under one conjunctive schedule (conjunctive fixed-interval fixed-ratio schedule), a response was reinforced after a 6-min interval had elapsedand a specific minimum number of responses had been emitted, Under a second conjunctive schedule, a response was reinforced after the 6-min fixed interval and upon completion of a tandem schedule requirement (conjunctive fixed-interval tandem schedule), This schedule retained the same required minimum number of responses as the first conjunctive schedule, but responses were never reinforced according to a fixed-ratio schedule; the tandem schedule was comprised of a fixed-ratio and a small (.1 to 10.0 sec) fixed-interval schedule, Under the conjunctive fixed-interval fixed-ratio schedule, responding was characterized by an initial pause, an abrupt transition to a high response rate, and a second transition to a lower rate that prevailed or slightly increased up to reinforcement, Under the conjunctive fixed-interval tandem schedule, pauses were extended, response rates were lower, and the initial high rate of responding was generally absent, The above effects depended upon the size of the fixed interval of the tandem schedule, The distinct pattern of responding generated by conjunctive fixed-interval fixed-ratio schedules depends upon occasional reinforcement of fixed-ratio responding and not merely on the addition of a minimum number of required responses. 相似文献
5.
In three experiments, we examined the effect on the patterns of responding noted on fixed interval (FI) schedules of prior
exposure to a range of interval and ratio schedules. Rats leverpressed for food reinforcement on random ratio (RR), random
interval (RI), or variable interval (VI) schedules prior to transfer to FI schedules. In Experiment 1, prior exposure to an
RR schedule retarded the development of typical FI patterns of responding. Exposure to a yoked RI schedule produced even greater
retardation of typical FI performance. This effect was replicated in Experiment 2, using a within-subjects design. Rats responded
on a multiple RR-RI schedule prior to a multiple FI-FI schedule. Typical FI performance emerged more slowly in the component
previously associated with the RI than with that associated with the RR. In Experiment 3, exposure to an RR schedule retarded
the development of FI performance to a greater extent than did exposure to a VR schedule. The latter schedule was programmed
to allow the possibility that inhibitory control would develop after reinforcement. These results confirm that ratio schedules
independently result in the disruption of FI responding. This effect was not long lasting and cannot be used plausibly to
explain species differences in responding to FI schedules. However, it does suggest that temporal control—as manifested by
the transfer of inhibitory control from one schedule to another—could facilitate movement between interval schedules. 相似文献
6.
Frances K. McSweeney 《Learning & behavior》1975,3(3):264-270
Five pigeons pecked for food reinforcement on several concurrent schedules. Their body weights were varied from 80% to 110% of their free-feeding weights. A number of predictions of the equations proposed by Herrnstein (1970) were tested. As predicted, the relative rate of responding equalled the relative rate of reinforcement for all subjects, on all schedules, at all body weights. And, as predicted, the overall rates of responding on the components of a concurrent schedule were slower than the local rates of responding on the components of an identical multiple schedule. Contrary to prediction, the total rate of responding generated by the concurrent schedules did not increase with increases in the total rate of reinforcement they provided. And, contrary to prediction, the k parameter did not remain constant, and the R0 parameter did not increase with increases in body weight. It was concluded that Herrnstein’s matching law and his interpretation of the m parameter are correct but that the interpretations of k and R0 require further investigation. 相似文献
7.
Frances K. McSweeney 《Learning & behavior》1978,6(4):444-450
Four pigeons pecked keys and pressed treadles for food reinforcers delivered by several variable-interval schedules of reinforcement. Then the subjects responded on several concurrent schedules. Keypecking produced reinforcers in one component, and treadle-pressing produced reinforcers in the other. The changeover delay, which prevented reinforcement after all switches from one response to the other, was 0, 5, or 20 sec long. An equation proposed by Kerrnstein (1970) described the rates of treadle-pressing and keypecking emitted during the variable-interval schedules. The k parameter of this equation was larger for keypecking than for treadle-pressing. The R0 parameters were not systematically different for the two responses. The rates of keypecking and treadle-pressing emitted during the components of the concurrent schedules correlated with, but were not equal to, the rates of responding predicted by Herrnstein’s equation and the subject’s simple schedule responding. The ratios of the rates of responding emitted during, and the ratios of the time spent responding on, the components of the concurrent schedules conformed to an equation proposed by Baum (1974), but not to Herrnstein’s equation. 相似文献
8.
Frances K. McSweeney 《Learning & behavior》1980,8(3):392-400
Pigeons pecked keys for food reinforcers delivered by several variable-interval and multiple variable-interval schedules. The rates of responding emitted during the simple schedules were not systematically different from the rates emitted during the multiple schedules when the components of the multiple schedule were identical. The rates of responding emitted during the components were usually greater than the rates emitted during comparable simple schedules when the components were more favorable than the added components of the multiple schedules. Response rates during the components were not significantly lower than those during comparable simple schedules when the components were less favorable. The observation of higher rates of responding during the more favorable components conforms to a prediction of several additive theories (e.g., Rachlin, 1973) but violates a prediction of Herrnstein’s (1970) theory. However, the additive theories are brought into question by the fact that changing the location of the discriminative stimuli did not change the pattern of results. 相似文献
9.
The aim of the four present experiments was to explore how different schedules of reinforcement influence schedule-induced
behavior, their impact on evaluative ratings given to conditioned stimuli associated with each schedule through evaluative
conditioning, and the transfer of these evaluations through derived stimulus networks. Experiment 1 compared two contrasting
response reinforcement rules (variable ratio [VR], variable interval [VI]). Experiment 2 varied the response to reinforcement
rule between two schedules but equated the outcome to response rate (differential reinforcement of high rate [DRH] vs. VR).
Experiment 3 compared molar and molecular aspects of contingencies of reinforcement (tandem VIVR vs. tandem VRVI). Finally,
Experiment 4 employed schedules that induced low rates of responding to determine whether, under these circumstances, responses
were more sensitive to the molecular aspects of a schedule (differential reinforcement of low rate [DRL] vs. VI). The findings
suggest that the transfer of evaluative functions is determined mainly by differences in response rate between the schedules
and the molar aspects of the schedules. However, when neither schedule was based on a strong response reinforcement rule,
the transfer of evaluative judgments came under the control of the molecular aspects of the schedule. 相似文献
10.
Pigeons’ choice responding on 10-sec interpolated probes was studied after baseline training on multiple variable-interval variable-interval schedules of food reinforcement. Unreinforced choice following training with three different relative reinforcement rates (Experiment 1), with a 3-ply multiple schedule (Experiment 2), and with three different relative reinforcement durations (Experiment 3) was examined. Least squares lines were fit to choice relative response rate and schedule relative response rate as functions of training relative reinforcement rate; choice slope was significantly greater than schedule slope in all three experiments. This result is counter to the prediction of Herrnstein’s (1970) theory that these slopes should not differ. Luce’s (1959) theory also failed to account for the data. It was concluded that choice responding was controlled by both approach to the stimulus associated with the smaller mean interreinforcer interval or the longer duration, and avoidance of the other stimulus. 相似文献
11.
Terry W. Belke 《Learning & behavior》1992,20(4):401-406
Four pigeons were exposed to multiple schedules with concurrent variable interval (VI) components and then tested for preference transfer. Half of the pigeons were trained on a multiple concurrent VI 20-sec, VI 40-sec/cuncurrent VI 4G-sec5 VI 80-sec schedule. The remaining pigeons were trained on a multiple concurrent VI 80-sec, VI 40-sec/concurrent VI 40-sec, VI 20-sec schedule-After stability criteria for time and response proportions were simultaneously met, four preference transfer tests were conducted with the stimuli associated with the VI 40-sec schedules. During the transfer tests, each pigeon allocated a greater proportion of responses (M=0,79) and time (M=0.82) to the stimulus associated with the VI 40-sec schedule that was paired with the VI 80-sec schedule than lo the VI 40-sec schedule stimulus paired with the VI 20-sec schedule. Absolute reinforcement rates on the two VI 40 sec schedules were approximately equal and unlikely to account for the observed preference. Nor was the preference consistent with the differences in local reinforcement rates associated with the two stimuli. Instead, the results were interpreted in terms of the differential value that stimuli acquire as a function of previous pairings with alternative schedules of reinforcement. 相似文献
12.
13.
Frances K. McSweeney 《Learning & behavior》1977,5(1):110-114
Four pigeons pecked for food reinforcers delivered by several two-key concurrent schedules. The sum of the rates of reinforcement provided by the component schedules varied from 25 to 300 reinforcers/h. The ratio of the rates of reinforcement remained constant at 1:4. The sum of the rates of responding generated by the component schedules increased with increases in the sum of the rates of reinforcement which the components provided. The increase in response rate was predicted by equations proposed by Catania (1963) and by Herrnstein (1970). But the data conformed more closely to Herrnstein’s equation. 相似文献
14.
Pigeons pecked keys on concurrent-chains schedules that provided a variable interval 30-sec schedule in the initial link.
One terminal link provided reinforcers in a fixed manner; the other provided reinforcers in a variable manner with the same
arithmetic mean as the fixed alternative. In Experiment 1, the terminal links provided fixed and variable interval schedules.
In Experiment 2, the terminal links provided reinforcers after a fixed or a variable delay following the response that produced
them. In Experiment 3, the terminal links provided reinforcers that were fixed or variable in size. Rate of reinforcement
was varied by changing the scheduled interreinforcer interval in the terminal link from 5 to 225 sec. The subjects usually
preferred the variable option in Experiments 1 and 2 but differed in preference in Experiment 3. The preference for variability
was usually stronger for lower (longer terminal links) than for higher (shorter terminal links) rates of reinforcement. Preference
did not change systematically with time in the session. Some aspects of these results are inconsistent with explanations for
the preference for variability in terms of scaling factors, scalar expectancy theory, risk-sensitive models of optimal foraging
theory, and habituation to the reinforcer. Initial-link response rates also changed within sessions when the schedules provided
high, but not low, rates of reinforcement. Within-session changes in responding were similar for the two initial links. These
similarities imply that habituation to the reinforcer is represented differently in theories of choice than are other variables
related to reinforcement. 相似文献
15.
In two experiments, food-deprived rat subjects leverpressed for food in three successive training phases. In the first phase of both experiments, rats were exposed to a multiple schedule, one component of which produced a high rate of response, and the other of which produced a lower rate of response (multiple random ratio [RR], random interval [RI] in Experiment 1, and multiple differential reinforcement of high rate, differential reinforcement of low rate in Experiment 2). Rats were then transferred to a multiple fixed interval (FI; 60-sec, 60-sec) schedule, until the effects of the first phase on response rate were no longer apparent and their response rates did not differ from those of rats responding on a multiple FI 60-sec, FI 60-sec schedule without previously experiencing a multiple RR, RI schedule. During the third stage oftraining, all rats were placed into extinction. During extinction, rates of responding were higher in the component previously associated with the high rate of responding in Phase 1, and they were lower in the component previously associated with low rates of responding in Phase 1. These results suggest that resurgence effects, like other history effects, are controlled by previous rates of responding. 相似文献
16.
Experiment 1 investigated the behavior of rats trained to leverpress on a concurrent variable ratio (VR) 30 VR-30 schedule with a brief, 500-msec, light occurring at the midpoint of the ratio on one of the levers. Higher response rates were recorded on the lever associated with this stimulus, a finding that paralleled the effect produced by inserting primary reinforcement at the midpoint (i.e., by training on a concurrent VR-30 VR-15 schedule). Similar results were found in Experiment 2 using a concurrent VR-20 VR-20 schedule with a 2-sec visual stimulus presented midway through one of the components. In addition, a brief stimulus inserted midway through the VR-20 component of a concurrent VR-20 VR-10 schedule retarded the development of a difference in response rates between the components relative to a VR-20 VR-10 group lacking the signal. In Experiment 3, multiple VR VR schedules were used. Again, the response rate was higher in the component that had the added stimulus or, for a second group of subjects, on the component with the smaller response requirement. Probe-choice trials revealed a preference for the component that generated the higher rate in both groups. Presenting a stimulus partway through a ratio appears to reduce the effect on response rate and choice of a large ratio value. 相似文献
17.
Three pigeons pecked keys for food reinforcers delivered by multiple variable interval variable interval schedules in the first part of each session (baseline) and by multiple variable interval extinction schedules in the second part of each session (contrast). The variable interval schedules delivered reinforcers after an average of 4 min or 30 sec in different conditions. The duration of a time-out between the components varied in five steps from 5 to 120 sec. Positive contrast occurred for all time-out durations in both experiments. That is, the rate of responding emitted during the constant, variable interval component was greater during the contrast than during the baseline schedules. The size of contrast did not change systematically with changes in timeout duration. These results violate most theories of contrast. They are compatible with the idea that animals integrate reinforcers over intervals longer than 2 min. 相似文献
18.
Roger M. Tarpy Jean E. Roberts Stephen E. G. Lea Marie Midgley 《Learning & behavior》1984,12(1):50-54
Previous research has shown that response rates on a variable interval (VI) schedule of reinforcement decrease if a brief response-produced signal is given prior to reward. One explanation is that the signal overshadows the response because it is a better predictor of reinforcement. The S-R overshadowing effect does not occur with variable ratio (VR) schedules, however. Tarpy, Lea, and Midgley (1983) explained this fact by suggesting that the signal functions to enhance the salience of the temporal interval offset on the VI schedule (a characteristic not possessed by VR schedules), which then overshadows the response. In this experiment, the salience of the temporal interval was enhanced in another way: signaled or unsignaled reward was provided to rats responding on either a VI or fixed interval (FI) reward schedule. As predicted, rates were lowest for animals receiving signaled reinforcement on an FI schedule and highest for those receiving unsignaled reinforcement on a VI schedule. 相似文献
19.
Five rats responded on several concurrent schedules in which pressing a key produced reinforcers in one component and pressing a lever produced reinforcers in the other component (Experiment 1). Four pigeons responded on several concurrent keypeck treadlepress schedules (Experiment 2). The programmed rates of reinforcement varied from 15 to 240 reinforcers per hour in different conditions. Rates of responding usually changed systematically within experimental sessions, and the changes were similar for the two components of a concurrent schedule. These results imply that within-session changes in responding may not confound the predictions of theories that describe the ratio of the rates of responding during the two components of concurrent schedules. Instead, within-session changes may be controlled by a mechanism that integrates the reinforcers obtained from the two components. 相似文献
20.
Phil Reed 《Learning & behavior》2016,44(1):78-84
An experiment examined the impact of a procedure designed to prevent response or extinction strain occurring on random interval schedules with a linear feedback loop (i.e., an RI+ schedule). Rats lever-pressed for food reinforcement on either a RI+ or a random interval (RI) schedule that was matched to the RI+ schedule in terms of reinforcement rate. Two groups of rats responded on an RI+ and two on an RI schedule matched for rate of reinforcement. One group on each schedule also received response-independent food if there had been no response for 60 s, and response-independent food continued to be delivered on an RT-60 schedule until a response was made. Rats on the RI and RI+ obtained similar rates of reinforcement and had similar reinforced inter-response times to one another. On the schedules without response-independent food, rats had similar rates of response to one another. However, while the delivery of response-independent food reduced rates of response on an RI schedule, they enhanced response rates on an RI+ schedule. These results suggest that rats can display sensitivity to the molar aspects of the free-operant contingency, when procedures are implemented to reduce the impact of factors such as extinction-strain. 相似文献